rs60336366
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs60336366(A;A) |
Make rs60336366(A;G) |
Make rs60336366(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 8 |
Position | 113650022 |
is a | snp |
is | mentioned by |
dbSNP | rs60336366 |
dbSNP (classic) | rs60336366 |
ClinGen | rs60336366 |
ebi | rs60336366 |
HLI | rs60336366 |
Exac | rs60336366 |
Gnomad | rs60336366 |
Varsome | rs60336366 |
LitVar | rs60336366 |
Map | rs60336366 |
PheGenI | rs60336366 |
Biobank | rs60336366 |
1000 genomes | rs60336366 |
hgdp | rs60336366 |
ensembl | rs60336366 |
geneview | rs60336366 |
scholar | rs60336366 |
rs60336366 | |
pharmgkb | rs60336366 |
gwascentral | rs60336366 |
openSNP | rs60336366 |
23andMe | rs60336366 |
SNPshot | rs60336366 |
SNPdbe | rs60336366 |
MSV3d | rs60336366 |
GWAS Ctlg | rs60336366 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24939585] |
Trait | Age-related hearing impairment |
Title | Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment. |
Risk Allele | |
P-val | 4E-6 |
Odds Ratio | .27 [NR] unit increase |